추천 제품
분석
97%
형태
solid
mp
>250 °C (dec.)
SMILES string
OC(=O)c1sc(C(O)=O)c2OCCCOc12
InChI
1S/C9H8O6S/c10-8(11)6-4-5(7(16-6)9(12)13)15-3-1-2-14-4/h1-3H2,(H,10,11)(H,12,13)
InChI key
MCLQXEPXGNPDHG-UHFFFAOYSA-N
일반 설명
3,4-Propylenedioxythiophene-2,5-dicarboxylic acid (ProDOT) is an electron rich conducting polymer that can be used in organic and bio-electronics. It can functionalize a variety of polymers by enhancing the intrinsic properties.
애플리케이션
ProDOT is a conjugating polymer that can be used in the fabrication of a variety of organic electronics which include electrochromic devices, lithium ion batteries, and organic semiconductors.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Conducting poly (3, 4-alkylenedioxythiophene) derivatives as fast electrochromics with high-contrast ratios.
Chemistry of Materials, 10(3), 896-902 (1998)
Propylenedioxythiophene (ProDOT)-phenylene copolymers allow a yellow-to-transmissive electrochrome.
Polym. Chem., 2(4), 812-814 (2011)
Multifunctional SA-PProDOT binder for lithium ion batteries.
Nano Letters, 15(7), 4440-4447 (2015)
3, 4-Alkylenedioxy ring formation via double Mitsunobu reactions: an efficient route for the synthesis of 3, 4-ethylenedioxythiophene (EDOT) and 3, 4-propylenedioxythiophene (ProDOT) derivatives as monomers for electron-rich conducting polymers.
Chemical Communications (Cambridge, England), 2498-2499 (2002)
Easy-to-make carboxylic acid dioxythiophene monomer (ProDOT-COOH) and functional conductive polymers.
Journal of Polymer Science Part A: Polymer Chemistry, 55(17), 2721-2724 (2017)
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